Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Ethnobotanical records document the use of Jasminum grandiflorum flowers as the primary plant part in traditional preparations across several cultures. In the Ayurvedic system of India, infusions of fresh or dried flowers are used to soothe mild respiratory ailments and as a calming nerve tonic, according to the *Indian Medicinal Plants Compendium* (Warrier et al., 1996). Among communities in the Middle East, particularly in Lebanon and Egypt, decoctions and strong infusions of the flowers are employed as an anti-inflammatory remedy, notably for skin irritations and mild digestive complaints, as described by Kamel et al. (2010) in their ethnobotanical survey. In parts of East Africa, notably Kenya and Tanzania, macerations of the crushed flowers are applied topically as poultices for wound healing and minor burns, with documented use by Kamba and Gebauer (2018). European herbal traditions, especially in the French pharmacopeia, recognize the flowers' use in mild sedatives, prepared as infusions for nervous tension (Blumenthal et al., 1998).

For a practical preparation, a simple calming infusion involves steeping 1 to 2 teaspoons (approximately 1-2 grams) of dried jasmine flowers in 240 ml (1 cup) of freshly boiled water, covered, for 8-12 minutes. For a stronger topical application, a decoction can be made by simmering 2 tablespoons (about 5 grams) of dried flowers in 250 ml of water for 10 minutes, cooling, and applying to affected areas with a clean cloth. A 1:5 ethanol tincture (1 part dried flowers to 5 parts 45% ethanol by weight) can be made with maceration for 4-6 weeks, shaking daily, before pressing and filtering; typical internal doses are 1-2 ml, 2-3 times daily. Cautions include potential allergic reactions; internal use should be moderate, and use during pregnancy or lactation is generally not recommended without professional guidance (Bown, 2001).

The relaxing and mildly analgesic effects of *Jasminum grandiflorum* are attributed to well-established aromatic constituents present in the flowers, primarily the monoterpenes linalool and linalyl acetate, along with the phenylpropanoid compounds benzyl acetate and eugenol (Weyerstahl et al., 1994). These volatile oils are responsible for the characteristic fragrance and possess documented sedative and anti-inflammatory properties that align with traditional use. While human clinical data remains limited, preliminary laboratory studies suggest antioxidant potential.

Modern relevance includes ongoing research into its essential oil for anxiolytic applications and continued traditional use in certain herbal teas and aromatherapy products. It is commercially available for cultivation as an ornamental and for fragrance extraction.

General Uses Top

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Common products:
• Fresh flowers sold as cut ornamental material in the floral trade.
• Concrete and absolute obtained by solvent extraction of fresh flowers; the absolute is the primary commercial fragrance product.

Industrial and craft applications:
• Solvent extraction and subsequent distillation of the concrete produce the absolute, which is incorporated as a fragrance ingredient in soaps, detergents, and consumer‑care products.
• The absolute is also used as a fixative and fragrance base in the manufacture of high‑end and niche perfumes.

Food and beverages (non‑medicinal):
• Jasmine absolute (Jasminum grandiflorum) is listed as a permitted flavoring in the United States (FEMA GRAS list) and under the EU Flavour Regulation (EC No 1334/2008).
• It imparts a characteristic floral aroma to jasmine‑scented tea blends, confectionery, and certain alcoholic beverages.

Fragrance and cosmetics:
• The absolute functions as a base‑note in perfume compositions, providing a rich, sweet floral scent.
• It is employed in lotions, creams, shampoos, and other personal‑care formulations as a fragrance and fixative.

Properties relevant to use:
• Major volatile constituents: benzyl acetate, linalool, jasmone, benzyl benzoate, and methyl jasmonate, which confer the characteristic odor.
• Typical physical data: specific gravity 0.92–0.95 (20 °C); refractive index 1.478–1.488; soluble in ethanol and diethyl ether, insoluble in water.
• Low acid value (

Synonyms Top

Scientific name	Authority	First published in
Jasminum hispanicum	hort. ex DC.	Prodr. 8: 313 (1844)
Jasminum catalonicum	hort. ex DC.	Prodr. 8: 313 (1844)
Jasminum officinale f. grandiflorum	(L.) Kobuski	J. Arnold Arbor. 12: 161 (1932)
Jasminum officinale var. grandiflorum	(L.) Stokes	Bot. Comm. 1: 21 1830
Jasminum grandiflorum var. plenum	Voigt	Hort. Suburb. Calcutt. 552. 1845
Jasminum officinale subsp. grandiflorum	(L.) E.Laguna	Toll Negre 8: 12 (2006)

Common names Top

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Filter by language:

Language	Common/alternative name
English	catalan jasmine
English	sicilian jasmine
English	spanish jasmine
English	royal jasmine
English	jasmine
English	jasmin
Spanish	jasminum officinale subsp. grandiflorum
Spanish	jasminum catalonicum
Spanish	jasminum hispanicum
Spanish	jasminum officinale f. grandiflorum
Spanish	jasminum officinale var. grandiflorum
Spanish	jasminum grandiflorum var. plenum
Arabic	ياسمين
Arabic	قانة
Arabic	ياسمين ابيض كبير الزهر
Arabic	ياسمين بستاني
Azerbaijani	İspaniya jasmini
Bengali	চামেলী (ফুল)
Bengali	চামেলি
Catalan	englantina
Catalan	j. grandiflorum
Catalan	gessamí
Estonian	suureõieline jasmiin
Persian	یاس اسپانیایی
Finnish	aitojasmiini
Gujarati	ચંપેલી
Hebrew	יסמין ספרדי
Hindi	चमेली
Indonesian	bunga pekan
Japanese	ソケイ
Kannada	ಜಾಜಿ
lzh	素馨
Malayalam	ജാസ് മിനം ഗ്രാന്റിഫ് ളോറം
Malayalam	പിച്ചകം
Malayalam	പിച്ചി
mnc	ᡤᡠᠸᠠᠩᡤᠠ ᡳᠯᡥᠠ
Marathi	जाई
Marathi	चमेली
Burmese	မြတ်လေးပန်း
Burmese	မုလေးပန်း
Norwegian Bokmål	storsjasmin
Nepali	चमेलि
Oriya	ଚାମେଲୀ
Punjabi	ਚਮੇਲੀ
Punjabi	ਚੰਬੇਲੀ
Punjab	چمیلی
Punjab	چنبیلی
Pashto	چامبېلي
sd	گل چين
sd	چَنبيلِي
Slovenian	velecvetni jasmin
Tamil	ஜாதி மல்லிகை வகை
Tamil	ஜாதி மல்லி வகை
Tamil	சாதி மல்லி வகை
Tamil	ஜாதி மல்லி
Tamil	சாதி மல்லி
Tamil	ஆசிய பெருமல்லி
Tamil	ஜாதி மல்லிகை
Tamil	சாதி மல்லிகை
Telugu	జాజి
Telugu	సన్నజాజి
Thai	มะลิก้านแดง
Chinese	荃皮
Chinese	素馨
Chinese	素馨花
Chinese	素馨子

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Jasminum grandiflorum subsp. floribundum	(R.Br. ex Fresen.) P.S.Green	Kew Bull. 41: 414 (1986)
Jasminum grandiflorum subsp. grandiflorum		Unknown

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Kenya
  - Uganda
- Northeast Tropical Africa
  - Djibouti
  - Eritrea
  - Ethiopia
  - Somalia
  - Sudan
- West Tropical Africa
  - Guinea
- West-central Tropical Africa
  - Rwanda
- Western Indian Ocean
  - Mauritius
  - Réunion

Asia-temperate click to expand
- Arabian Peninsula
  - Oman
  - Saudi Arabia
- China
  - China South-central

Asia-tropical click to expand
- Indian Subcontinent
  - Bangladesh
  - Maldives
  - Nepal
  - Pakistan
  - West Himalaya
- Malesia
  - Jawa

Northern America click to expand
- Mexico
  - Mexico Southeast

Pacific click to expand
- Northwestern Pacific
  - Marianas
- South-central Pacific
  - Cook Islands

Southern America click to expand
- Caribbean
  - Cuba
  - Dominican Republic
  - Haiti
  - Jamaica
  - Leeward Islands
  - Puerto Rico
  - Trinidad-Tobago
  - Windward Islands
- Central America
  - Belize
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
  - Nicaragua
  - Panamá
- Western South America
  - Bolivia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000813821
UNII	8DF4K1T8YO
Florida Plant Atlas	1455
Tropicos	23000153
INPN	104037
KEW	urn:lsid:ipni.org:names:328130-2
The Plant List	kew-351900
PFAF	Jasminum grandiflorum
Open Tree Of Life	783178
Observations.org	127139
NCBI Taxonomy	389181
IPNI	328130-2
iNaturalist	278277
GBIF	3172262
Freebase	/m/027yk7d
EPPO	IASOG
Elurikkus	5274
USDA GRIN	407300
Wikipedia	Jasminum_grandiflorum
CMAUP	NPO23178

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Methyl jasmonate ameliorates pain‐induced learning and memory impairments through regulating the expression of genes involved in neuroinflammation

Mohammadinia F, Esmaeili‐Mahani S, Abbasnejad M, Dogani M, Poorrahimi AM

Brain Behav

29-Apr-2024

PMCID:	PMC11056706
doi:	10.1002/brb3.3502
PMID:	38680072

Corythauma ayyari (Insecta, Heteroptera, Tingidae) depends on its host plant to spread in Europe

Durand M, Guilbert E

PLoS One

26-Mar-2024

PMCID:	PMC10965059
doi:	10.1371/journal.pone.0295102
PMID:	38530816

Phytocompounds targeting epigenetic modulations: an assessment in cancer

Khan A, Khan A, Khan MA, Malik Z, Massey S, Parveen R, Mustafa S, Shamsi A, Husain SA

Front Pharmacol

26-Mar-2024

PMCID:	PMC11002180
doi:	10.3389/fphar.2023.1273993
PMID:	38596245

Synthesis of eco-friendly layered double hydroxide and nanoemulsion for jasmine and peppermint oils and their larvicidal activities against Culex pipiens Linnaeus

Radwan IT, Khater HF, Mohammed SH, Khalil A, Farghali MA, Mahmoud MG, Selim A, Manaa EA, Bagato N, Baz MM

Sci Rep

22-Mar-2024

PMCID:	PMC10959945
doi:	10.1038/s41598-024-56802-y
PMID:	38519561

Empowering Strategies for Lifestyle Interventions, Diet Modifications, and Environmental Practices for Uterine Fibroid Prevention; Unveiling the LIFE UP Awareness

Vafaei S, Alkhrait S, Yang Q, Ali M, Al-Hendy A

Nutrients

12-Mar-2024

PMCID:	PMC10975324
doi:	10.3390/nu16060807
PMID:	38542717

Ethnobotanical study of traditional medicinal plants used by the local Gamo people in Boreda Abaya District, Gamo Zone, southern Ethiopia

Zemede J, Mekuria T, Ochieng CO, Onjalalaina GE, Hu GW

J Ethnobiol Ethnomed

28-Feb-2024

PMCID:	PMC10900619
doi:	10.1186/s13002-024-00666-z
PMID:	38419092

Use of Medicinal Plants in the Process of Wound Healing: A Literature Review

Cedillo-Cortezano M, Martinez-Cuevas LR, López JA, Barrera López IL, Escutia-Perez S, Petricevich VL

Pharmaceuticals (Basel)

27-Feb-2024

PMCID:	PMC10975678
doi:	10.3390/ph17030303
PMID:	38543089

Special Issue—“Natural Products That Might Change Society”

Amen Y, Shimizu K

Molecules

26-Feb-2024

PMCID:	PMC10934775
doi:	10.3390/molecules29051008
PMID:	38474520

Exotic and native plants play equally important roles in supporting and structuring plant-hummingbird networks within urban green spaces

Sánchez Sánchez M, Lara C

PeerJ

21-Feb-2024

PMCID:	PMC10893870
doi:	10.7717/peerj.16996
PMID:	38406283

Habitat suitability modelling of Koklass pheasant (Pucrasia macrolopha) in moist temperate forest

Badrulislam, Khan KA, Khalil S, Hussain M, Saqib Z, Altaf J, Hadi R, Habiba U

PLoS One

15-Feb-2024

PMCID:	PMC10868740
doi:	10.1371/journal.pone.0296921
PMID:	38359051

Management of the Brain: Essential Oils as Promising Neuroinflammation Modulator in Neurodegenerative Diseases

Avola R, Furnari AG, Graziano AC, Russo A, Cardile V

Antioxidants (Basel)

31-Jan-2024

PMCID:	PMC10886016
doi:	10.3390/antiox13020178
PMID:	38397776

Screening herbal extracts as biostimulant to increase germination, plant growth and secondary metabolite production in wheatgrass

Yadav A, Singh S, Yadav V

Sci Rep

05-Jan-2024

PMCID:	PMC10770375
doi:	10.1038/s41598-023-50513-6
PMID:	38182633

Understanding the Lost: Reconstruction of the Garden Design of Villa Peretti Montalto (Rome, Italy) for Urban Valorization

Bartoli F, D’Amato L, Nucera A, Albani Rocchetti G, Caneva G

Plants (Basel)

26-Dec-2023

PMCID:	PMC10780482
doi:	10.3390/plants13010077
PMID:	38202385

Oleuropein-Rich Jasminum Grandiflorum Flower Extract Regulates the LKB1-PGC-1α Axis Related to the Attenuation of Hepatocellular Lipid Dysmetabolism

Hou Y, Zhao X, Wang Y, Li Y, Chen C, Zhou X, Jin J, Ye J, Li D, Gan L, Wu R

Nutrients

24-Dec-2023

PMCID:	PMC10780778
doi:	10.3390/nu16010058
PMID:	38201888

Identification and Characterization of Jasmonic Acid Methyltransferase Involved in the Formation of Floral Methyl Jasmonate in Hedychium coronarium

Yue Y, Zhang X, Wang L, He J, Yang S, Li X, Yu Y, Yu R, Fan Y

Plants (Basel)

19-Dec-2023

PMCID:	PMC10780636
doi:	10.3390/plants13010008
PMID:	38202316

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	via CMAUP database
Protocatechuic Acid	72	Click to see	154.12	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.04.029
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
3-Methoxysalicylic acid	70140	Click to see	168.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
4-Methoxybenzoic Acid	7478	Click to see	152.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2,3-Dihydroxybenzoic Acid	19	Click to see	154.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol	244	Click to see	108.14	unknown	https://doi.org/10.1002/FFJ.2730010305
> Benzenoids / Benzene and substituted derivatives / Benzylethers
4-(2-Hydroxy-1-methoxyethyl)benzene-1,2-diol	22394752	Click to see	184.19	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.04.029
4-[(1S)-2-hydroxy-1-methoxyethyl]benzene-1,2-diol	86333779	Click to see COC(CO)C1=CC(=C(C=C1)O)O	184.19	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.04.029
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl acetate	8785	Click to see	150.17	unknown	https://doi.org/10.1002/FFJ.2730010305
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Hydron phenoxide	20488062	Click to see	94.11	unknown	via CMAUP database
> Benzenoids / Phenols / Cresols / Para cresols
P-Cresol	2879	Click to see	108.14	unknown	https://doi.org/10.1002/FFJ.2730010305
> Benzenoids / Phenols / Methoxyphenols
2-Methoxy-4-methylphenol	7144	Click to see CC1=CC(=C(C=C1)O)OC	138.16	unknown	https://doi.org/10.1002/HLCA.19630460330
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives
2-(3,4-dihydroxyphenyl)ethyl (E,3S)-4-formyl-3-(2-oxoethyl)hex-4-enoate	23624475	Click to see CC=C(C=O)C(CC=O)CC(=O)OCCC1=CC(=C(C=C1)O)O	320.30	unknown	https://doi.org/10.1055/S-2006-957419
3,4-Dihydroxyphenylethyl 4-formyl-3-formylmethyl-4-hexenoate	73117666	Click to see CC=C(C=O)C(CC=O)CC(=O)OCCC1=CC(=C(C=C1)O)O	320.30	unknown	https://doi.org/10.1055/S-2006-957419
Oleacein	18684078	Click to see	320.30	unknown	https://doi.org/10.1055/S-2006-957419
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Hydroxytyrosol	82755	Click to see	154.16	unknown	https://doi.org/10.1055/S-2006-957419 https://doi.org/10.1016/J.PHYTOCHEM.2007.04.029
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid	11005	Click to see	228.37	unknown	via CMAUP database
Oleic Acid	445639	Click to see	282.50	unknown	via CMAUP database
Palmitoleic Acid	445638	Click to see CCCCCCC=CCCCCCCCC(=O)O	254.41	unknown	via CMAUP database
Stearic Acid	5281	Click to see	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid	8215	Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O	340.60	unknown	via CMAUP database
Hexacosanoic Acid	10469	Click to see	396.70	unknown	via CMAUP database
Lignoceric Acid	11197	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O	368.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives / Jasmonic acids
(+)-7-iso-Jasmonic acid	7251183	Click to see CCC=CCC1C(CCC1=O)CC(=O)O	210.27	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2S,4aS,10aR)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-2-ol	13996029	Click to see CC(C)C1=CC2=C(C=C1)C3(CCC(C(C3CC2)(C)C)O)C	286.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(3R,4R,4aS,8aS)-4-[2-(furan-3-yl)ethyl]-4-hydroxy-3,4a,8,8-tetramethyl-2,3,5,6,7,8a-hexahydronaphthalen-1-one	101717490	Click to see	318.40	unknown	via CMAUP database
Rotundifuran	9841926	Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C	362.50	unknown	via CMAUP database
Vitetrifolin B	15543011	Click to see	362.50	unknown	via CMAUP database
Vitetrifolin C	15543012	Click to see	360.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol	442501	Click to see	154.25	unknown	via CMAUP database
(L)-alpha-terpineol	443162	Click to see	154.25	unknown	https://doi.org/10.1002/HLCA.19630460330
2-[(1S)-4-methylcyclohex-3-en-1-yl]propan-2-yl acetate	93317	Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C	196.29	unknown	via CMAUP database
Alpha-Terpineol	17100	Click to see	154.25	unknown	https://doi.org/10.1002/HLCA.19630460330
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
(+)-gamma-Tocopherol	92729	Click to see	416.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerone	92785	Click to see	424.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(Z)-methyl 4-(2-(3,4-dihydroxyphenethoxy)-2-oxoethyl)-3-ethylidene-2-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)-3,4-dihydro-2H-pyran-5-carboxylate	134688908	Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O	540.50	unknown	https://doi.org/10.21608/BFSA.2000.66313 https://doi.org/10.1055/S-2006-957419
2H-Pyran-4-acetic acid, 3-ethylidene-2-(beta-D-glucopyranosyloxy)-3,4-dihydro-5-(methoxycarbonyl)-, 2-(4-hydroxyphenyl)ethyl ester, [2S-(2alpha,3E,4beta)]-; Ligstroside	72727933	Click to see	524.50	unknown	https://doi.org/10.1248/CPB.47.1582
Demethyloleuropein	6450302	Click to see	526.50	unknown	https://doi.org/10.1248/CPB.47.1582
Ligstroside	14136859	Click to see	524.50	unknown	https://doi.org/10.1248/CPB.47.1582
methyl (4S,5E,6S)-4-[2-[(2R)-2-(3,4-dihydroxyphenyl)-2-methoxyethoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate	10769377	Click to see	570.50	unknown	https://doi.org/10.1248/CPB.47.1582
methyl (4S,5E,6S)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate	163186552	Click to see	540.50	unknown	https://doi.org/10.1055/S-2006-957419
methyl 4-[2-[2-(3,4-dihydroxyphenyl)-2-methoxyethoxy]-2-oxoethyl]-5-ethylidene-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate	85261819	Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC(C3=CC(=C(C=C3)O)O)OC	570.50	unknown	https://doi.org/10.1248/CPB.47.1582
methyl 4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxo-ethyl]-5-ethylidene-6-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-4H-pyran-3-carboxylate	3789874	Click to see	540.50	unknown	https://doi.org/10.1055/S-2006-957419 https://doi.org/10.1248/CPB.47.1582
Oleuropein	5281544	Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O	540.50	unknown	https://doi.org/10.1248/CPB.47.1582
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4AS,7S,7aS)-7-hydroxy-7-methyl-1-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(((4-hydroxybenzoyl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid	23955877	Click to see	496.50	unknown	via CMAUP database
CID 51346123	51346123	Click to see	466.40	unknown	via CMAUP database
Mussaenosidic acid	21633105	Click to see	376.36	unknown	via CMAUP database
Negundoside	9935561	Click to see	496.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(1R,3R,4R,4aS,8aS)-4-hydroxy-3,4a,8,8-tetramethyl-4-[2-(5-oxo-2H-furan-4-yl)ethyl]-2,3,5,6,7,8a-hexahydro-1H-naphthalen-1-yl] acetate	10022565	Click to see CC1CC(C2C(CCCC2(C1(CCC3=CCOC3=O)O)C)(C)C)OC(=O)C	378.50	unknown	via CMAUP database
3-[2-[(1R,2R,4aS,8aS)-1-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-2H-naphthalen-1-yl]ethyl]-2H-furan-5-one	102105798	Click to see CC1CCC2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C	320.50	unknown	via CMAUP database
Previtexilactone	21636179	Click to see	378.50	unknown	via CMAUP database
Vitexilactone	21636178	Click to see CC1CC(C2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C)OC(=O)C	378.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://doi.org/10.1055/S-2006-957419
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.04.029
3Alpha-Hydroxyurs-12-En-28-Oic Acid	7163177	Click to see	456.70	unknown	via CMAUP database
Alpha-Amyrin	73170	Click to see	426.70	unknown	via CMAUP database
Betulinic Acid	64971	Click to see	456.70	unknown	via CMAUP database
Corosolic Acid	6918774	Click to see	472.70	unknown	via CMAUP database
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
Oleanolic Acid	10494	Click to see	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.04.029
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)-	220774	Click to see	456.70	unknown	https://doi.org/10.1055/S-2006-957419
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(2E)-2-[(4aS,5R,7R,8R,8aS)-5-acetyloxy-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,5'-oxolane]-2'-ylidene]acetic acid	101357917	Click to see	364.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
trans-Jasmone	1549019	Click to see	164.24	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(3,4-Dihydroxyphenyl)-2-hydroxyethanone	22134444	Click to see C1=CC(=C(C=C1C(=O)CO)O)O	168.15	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.04.029
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Indole	798	Click to see	117.15	unknown	https://doi.org/10.1002/FFJ.2730010305
> Organoheterocyclic compounds / Lactones / Delta valerolactones
2-(2,6-Dioxooxan-4-yl)but-2-enal	73321500	Click to see	182.17	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.04.029
Jasminanhydride	16750859	Click to see	182.17	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.04.029
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Iso-ambreinolide	15559824	Click to see	264.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxocins
(6E,8aR,11aR)-1,4,5,8,8a,10,11,11a-octahydrocyclopenta[d]oxecine-2,9-dione	11106583	Click to see C1COC(=O)CC2CCC(=O)C2CC=C1	208.25	unknown	https://doi.org/10.1002/HLCA.19630460330
1,4,5,8,8a,10,11,11a-Octahydrocyclopenta[d]oxecine-2,9-dione	74817197	Click to see	208.25	unknown	https://doi.org/10.1002/HLCA.19630460330
> Organoheterocyclic compounds / Tetrahydrofurans
Vitex norditerpenoid 1	11208535	Click to see CC1CCC2C(CCCC2(C13CCC(=CC=O)O3)C)(C)C	290.40	unknown	via CMAUP database
Vitex norditerpenoid 2	11462191	Click to see	348.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-((2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl)-beta-D-glucopyranoside	132274946	Click to see	624.60	unknown	https://doi.org/10.1016/0031-9422(92)80178-H
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin	5280441	Click to see	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one	51402807	Click to see	464.40	unknown	https://doi.org/10.1055/S-2006-957419
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One	5378597	Click to see	464.40	unknown	https://doi.org/10.1055/S-2006-957419
Isoquercetin	5280804	Click to see	464.40	unknown	https://doi.org/10.1055/S-2006-957419
Rutin	5280805	Click to see	610.50	unknown	https://doi.org/10.21608/BFSA.2000.66313
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Bonanzin	5379563	Click to see	374.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin	5320351	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC	388.40	unknown	via CMAUP database
Casticin	5315263	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O	374.30	unknown	via CMAUP database
Chrysosplenol D	5280699	Click to see	360.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
12-(3,4-Dihydroxyphenyl)-20-ethylidene-16,17,18-trihydroxy-9-oxo-2,4,10,13,19-pentaoxatricyclo[13.3.1.13,7]icos-5-ene-6-carboxylic acid	73321499	Click to see	524.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.04.029
2'-Epifraxamoside	16750858	Click to see CC=C1C2CC(=O)OCC(OCC3C(C(C(C(O3)OC1OC=C2C(=O)O)O)O)O)C4=CC(=C(C=C4)O)O	524.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.04.029
2''-Epifraxamoside	11972585	Click to see	538.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.04.029
methyl (1S,3S,7S,12S,15S,16S,17S,18R,20E)-12-(3,4-dihydroxyphenyl)-20-ethylidene-16,17,18-trihydroxy-9-oxo-2,4,10,13,19-pentaoxatricyclo[13.3.1.13,7]icos-5-ene-6-carboxylate	162932872	Click to see CC=C1C2CC(=O)OCC(OCC3C(C(C(C(O3)OC1OC=C2C(=O)OC)O)O)O)C4=CC(=C(C=C4)O)O	538.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.04.029
Methyl 12-(3,4-dihydroxyphenyl)-20-ethylidene-16,17,18-trihydroxy-9-oxo-2,4,10,13,19-pentaoxatricyclo[13.3.1.13,7]icos-5-ene-6-carboxylate	73157825	Click to see	538.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.04.029

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Jasminum grandiflorum

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